📂 الأمراض
retinitis pigmentosa 18 — التعريف
Retinitis Pigmentosa 18 / retinitis pigmentosa 18
Retinitis pigmentosa 18 is a hereditary disease characterized by progressive degeneration of photoreceptor cells located in the retina of the eye. This situation starts with night blindness and peripheral vision loss, it can lead to harmony vision and full blindness in advanced stages. The disease shows autozomal resessive passage and is also known as RP18, usually associated with mutations in PRPF31 gene.
الأسئلة الشائعة
❓ ما هو Retinitis Pigmentosa 18؟
Retinitis Pigmentosa 18; retinitis pigmentosa 18 is a hereditary disease characterized by progressive degeneration of photoreceptor cells located in the retina of the eye. This situation starts with night blindness and peripheral vision loss, it can lead to harmony vision and full blindness in advanced stages. The disease shows autozomal resessive passage and is also known as RP18, usually associated with mutations in PRPF31 gene.
❓ ما معنى retinitis pigmentosa 18 بالتركية؟
المعادل التركي لـ "retinitis pigmentosa 18" هو Retinitis Pigmentosa 18.
❓ ما هو المجال الطبي الذي يتعلق بـ Retinitis Pigmentosa 18؟
هذا المصطلح ينتمي إلى فئة الأمراض.